Medical Device Manufacturer · US , Palo Alto , CA

Chestnut Medical Technologies, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2005

Recent clearances: ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX, MARKSMANN CATHETER, ALLIGATOR RETRIEVAL DEVICE (ARD)

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Chestnut Medical Technologies, Inc. Cardiovascular ✕

3 devices

1-3 of 3

Cleared Apr 22, 2010

ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX

Cardiovascular · 119d

Cleared Sep 18, 2009

MARKSMANN CATHETER

Cardiovascular · 113d

Cleared Mar 24, 2005

ALLIGATOR RETRIEVAL DEVICE (ARD)

Cardiovascular · 86d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 26, 2026